PX 53/15-BP, MODEL 130 050 AND PX 60/15-BP, MODEL 130 051


the company

Device Classification Name

permanent pacemaker electrode

510(k) Number K000763
Device Name PX 53/15-BP, MODEL 130 050 AND PX 60/15-BP, MODEL 130 051
Original Applicant
BIOTRONIK, GMBH & CO.
6024 jean rd.
lake oswego, 
OR 
97035

Original Contact jon brumbaugh
Regulation Number 870.3680
Classification Product Code
DTB  
Date Received 03/09/2000
Decision Date 04/06/2000
Decision

(ST)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

Type Special
Reviewed by Third Party No

Combination Product

No